The general purpose of the study is to evaluate the potential beneficial effects of PEA 600 mg supplementation on RGCs function in subjects with glaucoma by pattern electroretinogram after three months of therapy. Secondary objectives are to assess effects on intraocular pressure (IOP) values, if any; to record visual acuity, visual field, central corneal thickness (CCT), and Optical coherence tomography (OCT) (ganglion cell complex - GCC) changes, if any and to follow quality of life (QL) perception (general vision -GV and general health - GH of national eye instutute visual functioning questionnaire 25 items - NEI VFQ25)
Monocentric, randomized, prospective, single blind, two treatment and two period crossover study. The investigators have proposed a cross-over trial to avoid or to detect the bias due to intra-individual variability and because, from preliminary observation, it has been noted that the effects of PEA on pattern-electroretinogram (PERG) are completely reversible after withdrawal, within one month. The investigators didn't considered a placebo treated group because the patient cannot interfere with the pattern-electroretinogram PERG measurement that is objective and totally patient-independent. Study duration 12 months Enrolment period 6 months Minimum Follow-up 6 months Start: January, 2015; end January, 2016 Total sample size: 40 patients
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
DOUBLE
Enrollment
40
PEA 600 mg was added to topical therapy
To assess effects of PEA 600 mg a tablet a day on pattern electroretinogram PERG examination at three months of therapy.
changes in amplitude (microVolt) and changes in latency (millisecond) of p50 and n95 waves
Time frame: 3 months
To assess effects of PEA 600 mg on intraocular pressure (IOP) values
IOP measure in mmHg
Time frame: 3 months
To record visual field changes
changes in MD (deciBell-dB) and pattern standard deviation-PSD (deciBell-dB) of visual field parameters
Time frame: 3 months
To follow quality of life - QL - perception using the 25 item National Eye Institute - Visual Functioning Questionnaire (NEI VFQ25)
changes in the total mean score, in the General vision -GV- and in the general health -GH- subscales scores (scores are presented as a number, higher numbers reflect higher QL)
Time frame: 3 months
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